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    <responseDate>2026-10-14T19:46:38Z</responseDate>
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    <identifier>10.57760/sciencedb.33696</identifier>
    <datestamp>2026-01-07T09:49:32Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-01-07</dc:date>
  <dc:title>High-Altitude Hypoxia Triggers JNK Phosphorylation: A Molecular Switch Linking Hippocampal Energy Crisis, Neuronal Senescence, and Cognitive Impairment</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.33696</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>This dataset supports the study of &amp;quot;Chronic high-altitude hypoxia drives cognitive impairment, mitochondrial dysfunction, and cellular aging by activating the hippocampal JNK-P53 axis&amp;quot;. Samples were collected at multiple time points using a chronic low-pressure hypoxia rat model (simulating an altitude of 6000m), covering: (1) epidemiological statistical data of 2819 populations in areas above 3000m altitude; (2) Western blot was used to detect the expression and phosphorylation levels of JNK/p53/Bim and other proteins; (3) LC-MS/MS untargeted metabolomics analysis; (4) Immunofluorescence staining (LAMP1/COVIV and PHD2/HIF-2 &amp;alpha;); (5) Observation of transmission electron microscopy ultrastructure; (6) Morris water maze spatial memory test; (7) Morphological analysis of hippocampal CA1 region using HE staining. Statistical analysis was conducted using GraphPad Prism 10.1 for multiple sample comparisons (t-test/U-test/ANOVA/Kruskal Wallis et al.), while metabolomics was processed using MSDIAL 4.9 and differential metabolites were screened using Wilcoxon/ANOVA combined with VIP&amp;gt;1 and FC &amp;ge; 1.5 (FDR corrected p&amp;lt;0.05). The dataset is shared using CC BY 4.0 protocol.&amp;nbsp;</dc:description>
  <dc:subject>High-altitude hypoxia; JNK-P53 axis; Cognitive impairment; Mitochondrial dysfunction; Cellular senescence</dc:subject>
  <dc:creator>Hao Guisheng</dc:creator>
  <dc:creator>Jin Guoen</dc:creator>
  <dc:creator>Rili Ge</dc:creator>
  <dc:rights>EMBARGO</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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